Canonical Allele Identifier: CA2758363816
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529254_129529255insAA , CM000665.2:g.129529254_129529255insAA GRCh38
NC_000003.11:g.129248097_129248098insAA , CM000665.1:g.129248097_129248098insAA GRCh37
NC_000003.10:g.130730787_130730788insAA NCBI36
NG_009115.1:g.5616_5617insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+160_361+161insAA MANE Select ENSP00000296271.3:n.361+160_361+161insAA
ENST00000296271.3:c.361+160_361+161insAA ENSP00000296271.3:n.361+160_361+161insAA
NM_000539.3:c.361+160_361+161insAA MANE Select NP_000530.1:n.361+160_361+161insAA